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Thrombocytosis clinical trials

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NCT ID: NCT01163110 Completed - Cancer Clinical Trials

Study to Investigate the Therapeutic Role of RNA Fragments in Platelet Production During Chemotherapy

Start date: March 2004
Phase: Phase 1
Study type: Interventional

The purpose of this study is to measure the therapeutic potential of Escherichia coli (E. coli) and yeast ribosomal Ribonucleic acid (RNA) fragments to maintain the production of platelets in patients undergoing cytotoxic therapy for cancer.

NCT ID: NCT01147809 Completed - Thrombocytopaenia Clinical Trials

Safety and Efficacy Study for Solid Tumor Patients Treated With Eltrombopag

Start date: June 2010
Phase: Phase 2
Study type: Interventional

The present study is a randomized, blinded, placebo-controlled, two-Phase, sequential cohort, dose finding study to assess the safety and efficacy of eltrombopag in patients with solid tumors receiving gemcitabine monotherapy or the combination of gemcitabine plus carboplatin or cisplatin. Phase I of the study will examine safety and tolerability of various doses of eltrombopag to identify a dose and schedule of eltrombopag. Phase II will confirm that the chosen dose and schedule of eltrombopag from Phase I can deliver clinically meaningful benefit(s) to thrombocytopenic patients by improving platelet numbers.

NCT ID: NCT01134120 Completed - Clinical trials for Primary Myelofibrosis

A Study in Myeloproliferative Disorders

Start date: April 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find out the safe dose range of the study drug in patients with myeloproliferative disorders.

NCT ID: NCT01065038 Completed - Clinical trials for Essential Thrombocythaemia

Anagrelide vs. Hydroxyurea - Efficacy and Tolerability Study in Patients With Essential Thrombocythaemia

ANAHYDRET
Start date: September 2002
Phase: Phase 3
Study type: Interventional

Study AOP 03-007 was designed as a pivotal study to test, if Anagrelide (Thromboreductin®)was not inferior to HU with respect to efficacy in patients with ET. This approach to demonstrate non-inferiority was based on the following decision points: • ET is a rare disease and recruitment of large patient number (> 1600) to prove superiority was not considered possible. . It was decided to recruit only treatment naïve high risk patients to avoid pre-treatment bias, which further limited the number of patients eligible for the study.

NCT ID: NCT01053494 Completed - Clinical trials for Chronic Myelomonocytic Leukemia

Massage Therapy Given by Caregiver in Treating Quality of Life of Young Patients Undergoing Treatment for Cancer

Start date: April 2010
Phase: N/A
Study type: Interventional

This clinical trial studies massage therapy given by caregiver in treating quality of life of young patients undergoing treatment for cancer. Massage therapy given by a caregiver may improve the quality of life of young patients undergoing treatment for cancer

NCT ID: NCT01013181 Completed - Thrombopenia Clinical Trials

Safety and Efficacy of Romiplostim in Immune Thrombocytopenia (ITP) in the " Real-life " : Result of the French Experience in 72 Adults

ATU-r
Start date: January 2008
Phase: N/A
Study type: Observational

The purpose of this study is to review the charts of the first 100 patients included in the french compassionate program including patients with Immune Thrombopenia receiving romiplostim.

NCT ID: NCT00948792 Completed - Thrombocytopenia Clinical Trials

Study of the Effect of Differing Platelet Transfusion Times in Neonates

Start date: May 2009
Phase: N/A
Study type: Interventional

To evaluate changes in platelet counts and hemodynamics between "rapid" and "long" platelet infusion groups.

NCT ID: NCT00946270 Completed - Polycythemia Vera Clinical Trials

Pomalidomide for Myelofibrosis Patients

Start date: July 22, 2009
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if CC-4047 (now called pomalidomide) and prednisone can help to control MMM. The safety of this therapy will also be studied.

NCT ID: NCT00935987 Completed - Clinical trials for Primary Myelofibrosis

Safety and Efficacy Study of CYT387 in Primary Myelofibrosis (PMF) or Post-polycythemia Vera (PV) or Post-essential Thrombocythemia (ET)

Start date: November 2009
Phase: Phase 1/Phase 2
Study type: Interventional

This study seeks to (i) determine a safe and tolerated dose of CYT387 (momelotinib) given to patients with PMF, post-PV or post-ET and, (ii) assess the effectiveness of orally-administered CYT387 as a treatment for PMF, post-PV or post-ET.

NCT ID: NCT00925236 Completed - Clinical trials for Fechtner Syndrome (Disorder)

Phenotypic and Genotypic Identification and Characterization of MYH9-related Constitutional Thrombocytopenia

MAGIC-MYH9
Start date: August 2009
Phase: N/A
Study type: Observational

The research involves the establishment of a cohort including as much as possible cases of macrothrombocytopenia related to a "MYH9 syndrome" and the study of mutations and polymorphisms of MYH9 gene in all these patients. As MYH9 syndrome is an autosomal dominant disorder, patients should be heterozygous for a MYH9 gene mutation. The main goal of our project is looking for correlations between genotype and phenotype. It is planned to characterize the phenotype and genotype of a cohort of patients, including family members that will be addressed during the study in order to better understand the platelet disorder and improve the epidemiological knowledge of MYH9 syndrome. The data will be recorded in a database.